Surgical Filament Snare Assemblies

ABSTRACT

A surgical filament snare assembly including an anchor capable of being fixated in bone and having a filament engagement feature. A first filament has a noose with first and second noose limbs connected, preferably slidably connected, to the filament engagement feature of the anchor. The first and second noose limbs emerge from the anchor as first and second free filament limbs which are capable of being passed through tissue to be repaired and then passable through the noose. The noose, such as one or more half-hitches, is capable of receiving the free filament limbs and strangulating them when tension is applied to at least one of the free filament limbs and the noose to enable incremental tensioning of the tissue after the anchor is fixated. Preferably, the snare assembly further includes a flexible sleeve joining at least some portion of the first and second free filament limbs to facilitate passing of the free filament limbs at least through the tissue as a single unit.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims priority to and is a divisional of U.S.patent application Ser. No. 13/435,834, filed Mar. 30, 2012, andentitled “SURGICAL FILAMENT SNARE ASSEMBLIES,” which is a continuationof U.S. patent application Ser. No. 13/218,810, filed Aug. 26, 2011, andentitled “SURGICAL FILAMENT SNARE ASSEMBLIES,” which is a continuationin part of U.S. patent application Ser. No. 12/977,154, filed Dec. 23,2010, and entitled “SURGICAL FILAMENT SNARE ASSEMBLIES,” which is anon-provisional of U.S. Provisional Application No. 61/416,562, filedNov. 23, 2010, and entitled “TISSUE ANCHOR WITH FRICTIONAL SUTUREENGAGEMENT, each of which is hereby incorporated by reference in itsentirety. U.S. patent application Ser. No. 13/218,810, filed Aug. 26,2011, and entitled “SURGICAL FILAMENT SNARE ASSEMBLIES,” is also acontinuation in part of U.S. patent application Ser. No. 12/977,146,filed Dec. 23, 2010, and entitled “ADJUSTABLE ANCHOR SYSTEMS ANDMETHODS,” which is also hereby incorporated by reference in itsentirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention relates to filament assemblies for securing tissue to boneand more particularly to adjustable tensioning of tissue independent ofanchor fixation.

2. Description of the Related Art

A common injury, especially among athletes, is the complete or partialdetachment of tendons, ligaments or other soft tissues from bone. Tissuedetachment may occur during a fall, by overexertion, or for a variety ofother reasons. Surgical intervention is often needed, particularly whentissue is completely detached from its associated bone. Currentlyavailable devices for tissue attachment include screws, staples, sutureanchors and tacks.

Arthroscopic knot tying is commonly practiced in shoulder rotator cuffand instability procedures. Typically, an anchor loaded with suture isattached to bone first. The suture is normally slidably attached to theanchor through an eyelet or around a post, such that a single length ofsuture has two free limbs. One limb of the suture is passed through softtissue to be repaired such as a tendon or labrum. The two ends of thesuture are then tied to each other, thereby capturing the soft tissue ina loop with the anchor. Upon tightening the loop, the soft tissue isapproximated to the bone via the anchor.

Surgeons typically tie the suture ends by first placing a surgicalsliding knot such as the Tennessee Slider or Duncan Knot. Aftertightening the loop, a number of additional half hitches or other knotsare tied. The additional knots are needed because a conventional slidingknot does not provide the necessary protection against loosening orslippage, especially when tension is placed primarily on the limbs ofthe loop. Generally accepted practice is to follow the sliding knot withat least three reversed half hitches on alternating posts of the suture.

Before one or more half hitches or other knots can be added to thesliding knot, however, there exists a potential for the sliding knot toslip, that is, for the loop to enlarge as the tissue places tension onthe loop. This has been referred to as “loop security” and canreportedly occur even in the hands of very experienced surgeons.Sometimes, even fully-tied knots may slip. Further, the overall size ofa conventional knot can be obstructive or intrusive, especially in tightjoints, which may damage cartilage or other tissue by abrasion with theknot.

Suture anchor systems with sliding and locking knots for repairing tornor damaged tissue include U.S. Pat. No. 6,767,037 by Wenstrom, Jr. Othersuture anchor systems suited especially for meniscal repair aredisclosed in U.S. Pat. No. 7,390,332 by Selvitelli et al. and areutilized in the OmniSpan™ meniscal repair system commercially availablefrom DePuy Mitek Inc., 325 Paramount Drive, Raynham, Mass. 02767.

There are a number of suture implant systems which proclaim to be“knotless”, that is, to not require a surgeon to tie a knot duringsurgery. Many such systems control tension on tissue by the depth towhich an anchor is driven into bone. U.S. Pat. Nos. 5,782,864 and7,381,213 by Lizardi disclose certain types of suture anchors whichcapture a fixed-length loop of suture. Adjustable loop knotless anchorassemblies utilizing an anchor element inserted into a sleeve aredescribed by Thal in U.S. Pat. Nos. 5,569,306 and 6,045,574 and in U.S.Patent Application Publication No. 2009/0138042. Other systems havingclamps or other locking mechanisms include U.S. Pat. No. 5,702,397 byGoble et al. and U.S. Patent Application Publication No. 2008/0091237 bySchwartz et al.

It is therefore desirable to have robust yet adjustable fixation oftissue while minimizing both the number and size of knots to be tied bya surgeon, especially during arthroscopic repair procedures.

SUMMARY OF THE INVENTION

An object of the present invention is to meet or exceed the tissuetension control and holding power of currently available suture anchorassemblies for tissue repair procedures while reducing the number ofhalf hitches or other knots to be tied by a surgeon.

Another object of the present invention is to reduce the size of thefinished knot for the assembly.

A still further object is to simplify the overall knot tying process forthe surgeon while providing enhanced loop security and knot security

Yet another object of the present invention is to provide incrementaltensioning after anchor fixation.

This invention features a surgical filament snare assembly including ananchor capable of being fixated in bone and having a filament engagementfeature. A first filament has a noose with first and second noose limbsconnected, preferably slidably connected, to the filament engagementfeature of the anchor. The first and second noose limbs emerge from theanchor as first and second free filament limbs which are capable ofbeing passed through tissue to be repaired and then passable through thenoose. The noose, such as one or more half-hitches, is capable ofreceiving the free filament limbs and strangulating them when tension isapplied to at least one of the free filament limbs and the noose toenable incremental tensioning of the tissue after the anchor is fixated.Preferably, the snare assembly further includes a flexible sleevejoining at least some portion of the first and second free filamentlimbs to facilitate passing of the free filament limbs at least throughthe tissue as a single unit.

In preferred embodiments, the sleeve is formed from a braided suture. Incertain embodiments, the first filament is a braided suture and asection of one of the first and second free filament limbs serves as thesleeve. In one embodiment, the sleeve section has fewer picks,preferably at least ten percent fewer, per unit length than the picksper unit length for the remainder of the first filament. In certainembodiments, the sleeve is positioned over the entire portion of thefirst and second filaments before implantation of the anchor in thepatient, and in some embodiments the sleeve is further positioned beyondthe filament engagement feature to cover at least some of the first andsecond noose limbs.

In some embodiments, the noose is retractable toward the anchor. A toolwith at least one projection such as a tube may be included to assistpassing the free filament limb through the noose. In certain embodimentswherein the noose is formed from at least one half hitch, the assemblyincludes at least two tubes capable of being removably inserted intodifferent loops of the half hitch to provide passages for two ends offree filament limbs. In some embodiments, the tubes are joined togetherand have at least one handle for manipulating the tubes. Preferably,each tube is slotted to facilitate removal of the free filament limbsfrom the tubes.

This invention may be expressed as a method of surgically repairingtissue, preferably utilizing a sleeve, by selecting an anchor capable ofbeing fixated in bone and having a filament engagement feature. A firstfilament is selected having a noose with first and second noose limbsconnected, preferably slidably connected, to the filament engagementfeature of the anchor. The first and second noose limbs emerge from theanchor as first and second free filament limbs which are capable ofbeing passed through tissue to be repaired and then passable through thenoose. Preferably a flexible sleeve, joining at least some portion ofthe first and second free filament limbs, is also selected to facilitatepassing of the free filament limbs at least through the tissue as asingle unit. The anchor is fixated in bone, and at least the sleeve ispassed through the tissue to be repaired. At least the free filamentlimbs, preferably with the sleeve, are passed through the noose. Thetissue is then tensioned as desired with the noose strangulating thefree filament limbs when tension is applied to at least one of the freefilament limbs and the noose to enable incremental tensioning of thetissue after the anchor is fixated. The sleeve is removed from thepatient.

This invention also features a surgical filament snare assembly havingan anchor capable of being fixated in bone and having a filamentengagement feature, and a first filament having a fixed-length loop,capable of being passed through tissue and capable of being formed intoa noose, on a first portion of at least a first limb and having a secondportion. The assembly further includes a second filament having acollapsible loop slidably attached to the second portion of the firstfilament, the collapsible loop being formed by a sliding knot with atensioning limb. The tensioning limb and the sliding knot are capable ofbeing passed through the noose to enable incremental tensioning of thetissue after the anchor is fixated in bone, with the noose strangulatingthe collapsible loop when tension is applied to at least one of the freesuture limb and the noose. At least one of the first filament and thesecond filament are slidably connected to the filament engagementfeature of the anchor.

In some embodiments, the first filament is formed as a continuous loop,and the collapsible loop is slidably connected to the filamentengagement feature.

This invention may also be expressed as a method of surgically repairingtissue with a fixed-length loop by selecting an anchor capable of beingfixated in bone and having a filament engagement feature. A firstfilament is selected having a fixed-length loop, capable of being passedthrough tissue to be repaired and capable of being formed into a noose,on a first portion of at least a first limb and having a second portionslidably attached to a collapsible loop of a second filament, thecollapsible loop being formed by a sliding knot with a tensioning limb,the tensioning limb and the sliding knot capable of being passed throughthe noose. The anchor is fixated in bone, and at least a portion of thefixed-length loop is passed through the tissue to be repaired. A portionof the fixed-length loop is formed into a Lark's Head knot to serve asthe noose. The tissue is then tensioned as desired with the noosestrangulating the collapsible loop when tension is applied to at leastone of the tensioning limb, the sliding knot and the noose to enableincremental tensioning of the tissue after the anchor is fixated.

This invention further features a surgical filament snare assembly witha bone anchor and a first filament having a noose, formed from at leastone half hitch, on a first portion of at least a first limb and having asecond portion connected to the filament engagement feature of theanchor. The noose is capable of receiving at least two free filamentlimbs and strangulating them when tension is applied to at least one ofthe free filament limbs and the noose. Preferably, the assembly furtherincludes a threader tool having at least two projections having distalends capable of being removably inserted into different loops of thehalf hitch. Each projection defines a channel capable of receiving aportion of at least one free filament limb to pass it through a loop ofthe half hitch, and each projection further defines a slot communicatingwith the channel to facilitate removal of the filament limb from thetool.

In certain embodiments, the projections are tubes joined together withat least one handle for manipulation the tube. The proximal ends of thechannels are connected by one of an intersection and a common passage,and the tool further includes a stop as a proximal portion of the one ofthe intersection and the common passage. In some embodiments, the stopis movable, and may include a spring to bias the stop toward theintersection or common passage. In yet other embodiments, the assemblyfurther includes at least two suture passers having distal ends forengaging portions of the free filament limbs, and the suture passerscapable of pulling the free filament limbs through the channels whenproximal-directed force is applied to proximal ends of the suturepassers.

This invention may yet also be expressed as a method of creating asurgical filament snare assembly by selecting a first filament havingfirst and second ends, and forming at least one half hitch with acentral opening in the first filament between the first and second ends.The first and second ends are passed through the central opening todefine a noose with first and second noose limbs, and the half hitch istightened to form a slidable knot for the noose. The first and secondfilament ends are passed through a filament engagement feature of ananchor to emerge from the anchor as first and second free filament limbswhich are capable of being passed through tissue to be repaired and thenpassable through the noose, the noose strangulating the free filamentlimbs when tension is applied to at least one of the free filament limbsand the noose opening.

BRIEF DESCRIPTION OF THE DRAWINGS

In what follows, preferred embodiments of the invention are explained inmore detail with reference to the drawings, in which:

FIG. 1 is a schematic side view of a surgical filament snare assemblyaccording to the present invention having an anchor and a noose;

FIG. 1A is a schematic side view of a hangman-type noose and FIG. 1B issuch a view of a half-hitch noose to be utilized according to thepresent invention;

FIG. 2 is a schematic side view of the assembly of FIG. 1 removablyconnected with a cannulated driver for initially fixating the anchorwith a threader loop passed through the noose;

FIGS. 3-10 are schematic side views illustrating a process for capturingand tensioning tissue to the surgical filament snare assembly accordingto the present invention, with FIG. 8A providing an example of a stopperknot shown in FIGS. 8, 9 and 10;

FIGS. 11 and 12 are perspective views of an alternative half-hitch noosein which multiple openings are utilized to strangulate two or more freefilament limbs;

FIG. 13 is a perspective view of tubes to assist threading of freefilament limbs through noose openings of FIG. 11;

FIG. 14A is a perspective view of a double-barreled, slotted threaderdevice;

FIG. 14B shows the device of FIG. 14A being utilized to thread a noose;

FIG. 15 is one exemplary embodiment of a snare assembly with aretractable-noose configuration according to the present invention;

FIG. 16 is another exemplary embodiment of a snare assembly with aretractable-noose configuration according to the present invention;

FIG. 16A is yet another exemplary embodiment of a snare assembly with aretractable-noose configuration according to the present invention;

FIG. 17 is still another exemplary embodiment of a snare assembly with aretractable-noose configuration according to the present invention;

FIG. 18 is another exemplary embodiment of a snare assembly with aretractable-noose configuration according to the present invention;

FIG. 19 is yet another exemplary embodiment of a snare assembly with aretractable-noose configuration according to the present invention;

FIG. 20 is a schematic top view of multiple filaments that are passedthrough a single noose of a snare assembly according to the presentinvention;

FIG. 21 is an enlarged view of one construction of the configurationshown in FIG. 18;

FIGS. 22-27 are sequential schematic side views illustrating oneexemplary embodiment of using the snare assembly of FIG. 18 with anotheranchor that is placed through tissue to be repaired;

FIG. 28 is a perspective view of a snare assembly according to thepresent invention having a cannulated suture anchor;

FIG. 29 is a schematic view of a filament having a snare formed as ahalf hitch plus an additional throw with first and second noose filamentlimbs extending therefrom, and one embodiment of a sleeve, indicated inphantom, according to the present invention covering some of the firstand second filament limbs;

FIGS. 30 and 31 are sequential views of the filament of FIG. 29 with thefree filament limbs being passed through the noose to form a cinchnoose, with a distal portion of a sleeve illustrated in FIG. 31;

FIG. 32 is a schematic side view of the filament and sleeve combinationof FIG. 29 implanted in a patient with an anchor;

FIG. 33 is a sketch of calculations for the relative lengths andpositions of filament limbs relative to a sleeve for certain embodimentsaccording to the present invention;

FIGS. 34-40 are schematic side views illustrating capture and tensioningof tissue utilizing another embodiment of sleeve and filament snareassembly according to the present invention;

FIG. 41 is a schematic side view of yet another sleeve and filamentsnare assembly according to the present invention;

FIGS. 42A-D are sequential schematic side views illustrating oneexemplary embodiment for constructing the snare assembly of FIG. 41;

FIGS. 43-46 are sequential schematic side views illustrating anotherexemplary embodiment of using the snare assembly of FIG. 41 to captiveand tension tissue;

FIGS. 47-50 are schematic side views of another snare assembly accordingto the present invention utilizing a lark's head knot, with FIG. 48Adepicting an alternative fixed-length loop;

FIG. 51 is a schematic top view of two suture passers, with the leftpasser placed diagonally over the right passer in preparation forbecoming intertwined;

FIG. 52 shows the suture passers of FIG. 51 after the distal end of theleft passer has been looped under and then over the right passer to forma simple half hitch;

FIG. 53 is a schematic top view of an improved threader tool accordingto the present invention with the suture passers of FIG. 52 held withinchannels by a fixed stop;

FIG. 53A is a side cross-sectional view along lines 53A-53A of FIG. 53;

FIG. 54 is a schematic side view of an alternative threader tool with amovable stop; and

FIGS. 55-57 are schematic top views of yet other threader toolsaccording to the present invention with different fixed-stopconfigurations.

DETAILED DESCRIPTION OF THE PRESENTLY PREFERRED EMBODIMENTS

This invention may be accomplished by a surgical filament snare assemblyincluding an anchor capable of being fixated in bone and having afilament engagement feature. A first filament has a noose, or a loopcapable of being formed into a noose, on a first, proximal portion of atleast a first limb and has a second portion connected, includingslidably or fixedly connected, directly or indirectly, to the filamentengagement feature of the anchor. The noose, such as one or morehalf-hitches, a Lark's Head knot, or a hangman-type noose, is capable ofreceiving at least one end of a free filament limb or a portion ofanother filament. The noose strangulates the free filament limb or otherfilament when tension is applied to the noose, to the free filamentlimb, and/or to the other filament.

In certain preferred constructions, at least a first free filament limb,which in some constructions is a length of the first filament and inother constructions is a second filament, is passed through tissue to berepaired and has at least one end passable through the noose to enableincremental tensioning of the tissue after the anchor is fixated inbone. The present application is directed to one or more improvementsdescribed below beginning with FIG. 29.

Surgical filament snare assembly 10, FIG. 1, has an anchor 12 and afirst filament 14. In this construction, anchor 12 defines an internalpassage 16 with a restricted opening 18 at its distal end 20 whichserves as a filament engagement feature. At least one bone-engagingfeature 22, such as an external rib or helical thread, is located on theouter surface of anchor 12 between distal end 20 and proximal end 24.

First filament 14 has a noose 30 at its proximal end and a fixed knot 32at the distal end of filament post or stem 15 which interacts withrestricted opening 18 to retain filament 14 in a fixed, permanentlyattached position. This arrangement may be referred to as the firstfilament 14 connected with the filament engagement feature 18, whichincludes the phrase passing through the filament engagement feature 18.Many conventional knots, such as a mulberry knot, can be utilized forfixed knot 32 as long as knot 32 has sufficient bulk to preventpull-through at clinically desired tensions on noose 30. A number ofother types of filament engagements are described below. Stem 15 is keptas short as possible to maintain noose 30 close to anchor 12 even afterit is collapsed as described below.

A well-known noose knot 33 is illustrated in FIG. 1A in which firstfilament 14 a has a hangman-type noose 30 a at its proximal end and afixed knot 32 a at the distal end of stem 15 a. Noose 30 a has slidingnoose knot 33 and defines an opening 34. Noose knot 33 is tied byforming a flattened “S” or “Z” shape at the proximal end of filament 14a to form a large proximal loop to serve as the noose opening and asmall loop spaced from the large loop. The doubled filament limbs arewrapped with the terminal end, also known as the working end. Aftertypically four to eight wrapping turns, the terminal end is tuckedthrough the small loop and trapped by pulling on whichever of the limbsof the large loop closes the small loop.

An alternative, simpler noose is illustrated for first filament 14 b,FIG. 1B, having a half hitch 35, also referred to as a simple oroverhand knot, tied to form noose 30 b in the middle of filament limbs36 and 38. Multiple openings are created by the loops in half hitch 35as described in more detail below, although central opening 37 is shownas a large single opening in FIG. 1B. First filament limbs 36 and 38 arefolded around half hitch 35 to form a double-stem arrangement, and thedistal ends of first filament limbs 36 and 38 are joined in knot 32 bafter being passed through a suitable filament engagement feature on ananchor.

Noose efficiency is defined herein as the strangulation strength perunit tension applied on the noose, either by pulling on the filament onwhich the noose is tied or which otherwise carries the noose, or bypulling on one or more strands or limbs of filaments passing through thenoose. A noose with lower internal friction in the noose knot will tendto have a higher noose efficiency.

One instrument for inserting anchor 12 into a hole drilled in bone isillustrated in FIG. 2. Driver 40 has a distal end 42 removablyinsertable into passage 16. Driver 40 is cannulated in this constructionand has a lumen 44 with an optional threader filament 46 that passesthrough noose 30. Use of a threader filament is optional, but may bedesirable when noose 30 is spaced only a short distance from filamentengagement feature 18, in other words, when noose 30 is initiallypositioned close to or inside of anchor 12.

In one procedure according to the present invention, anchor 12 is shownfixated within bone B, FIG. 3, after driver 40 has been removed, in ahole 50 spaced at a desired distance from tissue T to be repaired. Noose30 is in an initial open configuration. Threader filament 46 has asufficient length to have both a threader loop 52 on a first limb, and agraspable portion on a second limb 54, extend proximally above skin Swhile a mid-portion of threader filament 46 is slidably associated withnoose 30.

Continuing with this exemplary procedure, a second filament 60, FIG. 4,is threaded through tissue T using a suture passing instrument, aneedle, or other tissue-penetrating technique chosen by a surgeon. Bothfree filament limbs 62 and 64 are brought together, typically above skinS, or at least outside of a joint space, and passed through threaderloop 52, FIG. 5. Threader limb 54 is then pulled to thread both secondfilament limbs 62 and 64 through noose 30 as illustrated in FIG. 6 whilenoose 30 is in the initial open configuration. Alternatively, freefilament limbs 62 and 64 are passed directly through noose 30 withoutusing a threader filament.

When there is high noose efficiency, a light tug is sufficient tocollapse noose 30 on the filament limbs 62 and 64 as shown in FIG. 7 toprovide initial tensioning on the surgical filament snare assembly 10.Generally, a higher noose efficiency can be utilized when one or morefree filament limbs are threaded directly through noose 30 without usinga threader filament, or are threaded using a tube or threader devicesuch as shown in FIGS. 13-14B below.

After initial or pre-tensioning of free filament limbs 62 and 64, FIG.7, tension is released on limbs 62, 64 and a slidable stopper knot 70,FIG. 8, is tied by the surgeon on limbs 62, 64 above skin S An enlargedview of one construction for stopper knot 70 a, FIG. 8A, shows a halfhitch with an extra throw or turn, also known as a double overhand knot.A simple knot such as a single half hitch or overhand knot may besufficient for some situations. Other suitable, more robust surgeonslidable knots with higher load capacity include the Tennessee Sliderdescribed in the Arthroscopic Knot Tying Manual (2005) available fromDePuy Mitek, as well as the slidable, lockable knot by Wenstrom, Jr. inU.S. Pat. No. 6,767,037. Alternatively, a mechanical locking mechanismmay be utilized where overall profile is not critical, especially awayfrom a joint or other articulating surfaces.

Stopper knot 70 is advanced, typically using a knot pusher, until itcontacts noose 30, FIG. 9. Tension generated between tissue T and anchor12, alone or together with pulling on one of the filament limbs 62 or64, causes noose 30 to further collapse, FIG. 10, and strangulate thefilaments. Stopper knot 70 augments the strangulation by transferringall tissue-generated tension on the stopper knot to the noose 30 andpreventing slippage of filament limbs 62, 64 into the noose knot.Accordingly, a self-cinching mechanism is created which inhibitsloosening of the filaments. Tension can be increased incrementally in aratchet-like effect by further advancing the stopper knot or pulling onone of filament limbs 62, 64.

Once satisfactory tissue tension has been achieved, one or more halfhitches may be added to stopper knot 70 to fortify the loading capacityon the stopper knot and reduce the risk of loosening under adverseconditions. By comparison, conventional sliding knots typically arereinforced by at least two or three reversed half hitches placed onalternating posts. Due to the self-cinching effect of the presentinvention, fewer overall hitches or other knots are needed for stopperknot 70 to meet or exceed the load performance relative to conventionalknot systems. The present invention thereby accomplishes a lower overallknot profile to handle a given load. Limbs 62, 64 are trimmed asdesired. The stopper knot also minimizes fraying of the filament endsover time.

Preferred materials for filaments 14 and 60 include various surgicalsutures, typically size 0 to size 5, such as Orthocord™ suturecommercially available from DePuy Mitek, and Ethibond™ suture availablefrom Ethicon. Orthocord™ suture is approximately fifty-five tosixty-five percent PDS™ polydioxanone, which is bioabsorbable, and theremaining percent ultra high molecular weight polyethylene, whileEthibond™ suture is primarily high strength polyester. The amount andtype of bioabsorbable material, if any, utilized in the first or secondfilament is primarily a matter of surgeon preference for the particularsurgical procedure to be performed.

While the same type of suture, even identical suture, can be used forboth first, noose filament 14 and second, tissue filament 60, a suturehaving a lower abrasive property at its surface may be preferred by somesurgeons for second filament 60. The lower abrasive property can beachieved by a larger diameter, a softer composition, a softer braid,plait or strand pattern, or a combination of such characteristics. Theterm “braid” as utilized herein includes “plait” and other multifilamentpatterns.

The nooses illustrated in FIGS. 1-6 above have been described as havinga single opening through which one or more free filament limbs arethreaded. A simple half hitch or overhand-type “pretzel”-like knot isillustrated in FIG. 11 for noose 30 c having multiple useful openings80, 82 and 84. Side openings 80 and 84 are formed by minor loops 81 and83 of the half hitch knot in first filament limbs 36 c, 38 c whilecentral opening 82 is formed by the major loop. Free filament limbs 62 cand 64 c are shown in FIG. 12 extending through side opening 80 andcentral opening 82, respectively, although other combinations andpermutations, such as using side openings 80 and 84, or central opening82 and side opening 84, are also effective. Utilizing different areas orregions of the noose knot significantly increases effectivestrangulation and gripping on the free filament limbs. It is expectedthat utilizing multiple openings in the noose knot also minimizes anydependence of load carrying capacity on filament compliancecharacteristics. A simple, single half hitch stopper knot 70 c is alsoillustrated in FIG. 12.

While two or more threader filaments, or careful, potentially tediousmanipulation by a surgeon, could be utilized to achieve theconfiguration shown in FIG. 12, an alternative technique which avoidsinadvertent noose collapse is shown in FIG. 13. Tubes 90 and 92 haveouter diameters suitable for sliding into the side openings formed byloops 81 and 83. Filament limbs 36, 38 c are shown engaged with anchor12 c. Tubes 90 and 92 define passages 94 and 96, respectively, throughwhich free filament limbs 62 c and 64 c are threaded. Tubes 90 and 92are then disengaged from noose 30 c and drawn proximally along filamentlimbs 62 c and 64 c until they can be removed and discardedappropriately.

Double-barrelled threader device 100, FIG. 14A, has two threader tubes102, 104 which are joined together with a handle 106 and provide an eveneasier technique. In one construction, device 100 is molded as amonolithic unit using a polymer material. Tubes 102, 104 have internallumens 108, 110, respectively, also referred to herein as channels, withopenings at both ends as well as slots 112, 114, respectively, whichalso run the entire length of tubes 102, 104. During use, tubes 102, 104are placed through loops 81 d, 83 d, FIG. 14B, formed from firstfilament limbs 36 d, 38 d, and free filament limbs 62 d, 64 d areinserted through lumens 108, 110. Thereafter, limbs 62 d, 64 d aresimply lifted through slots 112, 114 to remove the fully-threadedfilaments from the device 100. One or more additional such tubes can beformed and utilized as desired. Also, the tubes 102, 104 can be formedas “C” or “U” shapes in cross-section, with wider slots thanillustrated.

There are a number of other configurations of snare assemblies accordingto the present invention which have one or more adjustable-length noosesupport stems or limbs that enable the noose to be retracted as desiredtoward an anchor. These configurations provide an additional level ofcontrol over the final filament positions and tensions. Snare assembly120, FIG. 15, has a noose 124 formed at one end of a first filament 122with a stem section 126 extending into anchor 130 to pass throughratchet-like one-way gate or clamping mechanism 132. The remainder offilament 122 serves as a limb 128, also referred to as a stem tail. Someexamples of one-way mechanisms are disclosed in U.S. Pat. No. 5,702,397by Goble et al., for example, which allow filament movement in only onedirection.

As illustrated in FIG. 15, anchor 130 is fixated in bone B. A secondfilament 134 is passed through tissue T and has free limbs 136 and 138passed through noose 124, initially positioned outside of a joint spacesurrounding tissue T. Limb 128, also positioned outside of the jointspace, is pulled to retract noose 124 toward mechanism 132. Typically,the noose 124 is collapsed, limb 128 is trimmed, and then a proceduresimilar to that illustrated for FIGS. 7-10 above is utilized.

Snare assembly 140, FIG. 16, has first filament 140 having a noose 144tied with two stem limbs 146 and 148 extending into anchor 150. In thisconstruction, anchor post 152 serves as a filament engagement feature toslidably attach filament 140 to anchor 150. Filament stem tail limbs154, 156 extend out of a joint space, together with noose 144 in aninitial configuration. Second filament 160 is passed through tissue Tand then free limbs 162, 164 are passed through noose 144 outside of thejoint space.

In the procedure illustrated in FIG. 16A, limbs 154 and 156 of firstfilament 142 are also passed through noose 144 and then pulled tocollapse noose 144 about all four limbs 154, 156, 162 and 164 and toretract noose 144 toward filament engagement post 152. One or moresliding knots are tied on limb pair 154, 156 of the stem tails to adjustthe proximity of noose 144 to the anchor 150 and then a simple knot istied on free limbs 162, 164 to adjust final tension on tissue T,although other combinations and permutations can be utilized within thescope of the present invention. Typically, the sliding knots arefinished with one or more half hitches to “seal” or complete thefixation.

Snare assembly 170, FIG. 17, utilizes a single filament 172 both tosecure noose 174 to anchor 180 and to tension tissue T. Stem limbs 176,178 pass into anchor 12 and slidably around filament engagement post 182to emerge from anchor 180 as tail limbs 184, 186 which are initiallykept out of the joint space, along with noose 174, when anchor 180 isfixated in bone B. In some constructions, anchor post 182 is an eyeletor a pulley pin. Free tail limbs 184, 186 are passed through tissue T,in the same or different places or regions, and then through noose 174.Noose 174 is collapsed and pulled into the joint space by applying lighttension to one, or preferably both, of the tail limbs 184, 186. A simplestopper knot is tied between tail limbs 184, 186 and pressed against thenoose 174 while tensioning the limbs 184, 186 to place a desired amountof tension on tissue T. The fixation is finalized by placing one or morehalf hitches against the stopper knot at noose 174.

Snare assembly 190, FIG. 18, has functional similarities to snareassembly 120, FIG. 15, but achieves ratchet-like noose retractionwithout one-way gate or clamping mechanisms. Filament 192, FIG. 18, hasa noose 194 with a stopper knot 196 at its terminal end to preventpull-through and to resist fraying. A sliding knot 198 enables loop 200,having loop limbs 202 and 204, to be shortened toward anchor 205 whenpost limb 206 is pulled. Loop 200 passes around anchor saddle or post207. This and other adjustable loop, sliding knot configurations aredescribed in more detail below in relation to FIGS. 21-27.

Snare assembly 310, FIG. 19, includes a first filament 302 with a noose304 and a loop 306 which is fixed in length, the overall length offilament 302 being subject to full collapse of noose 304. A secondfilament 316 has a terminal end 318, a sliding knot 322 retained at thedistal end of anchor 312, a post limb 320, and an adjustable loop 324formed by limbs 326, 328. This configuration is described in more detailbelow in relation to FIG. 28.

While most of the embodiments herein have been described in relation tosecuring one or two filament limbs passed through a single place orregion in a tissue T, this is not a limitation of the invention. Snareassembly 210, FIG. 20, has a first filament 211 with a noose 212 throughwhich pass free limbs 214, 216 and 218, 220 of second and thirdfilaments 222 and 224, respectively. Noose 212 is engaged by stem 213with anchor 215. Filaments 222 and 224 pass through tissue regions R1and R2, respectively. Multiple regions of a tissue, and potentiallymultiple types of sutures or other filaments, can thereby be securedusing a single snare assembly according to the present invention.

One arrangement of the filament 192 for snare assembly 190, FIG. 18, isillustrated in FIG. 21 for snare assembly 190 a. Noose 194 a is formedmerely by creating opening 232 in region 230 of filament 192 a andpassing filament 192 a through itself. Loop 200 a and sliding knot 198 aare formed thereafter on post limb 206 a. In this arrangement, anytension applied on stem 234, such as by pulling post limb 206 a, notonly collapses noose 194 a to strangulate objects passing through noose194 a, but also binds the portion of filament 192 a passing throughopening 232 upon itself. In other arrangements, a half hitch or othersimple knot is tied at filament region 230, and filament 192 a is thenlooped through that simple knot. Stopper knot 196 a such as a simplehalf hitch will prevent the terminal end from fraying or opening up,especially if a braided filament such as Orthocord™ suture is utilizedfor filament 192 a.

An example of steps for manufacturing snare assembly 190, FIG. 18,utilizing suture as filament 192 is as follows. Tie stopper knot 196 andtrim the tail of the terminal end. Loop the suture and pass it throughitself in close proximity to the stopper knot 196 to achieve the noosearrangement illustrated in FIG. 21, or tie a second half hitch in closeproximity to the stopper knot and pass the suture through the half hitchto create the noose 194, FIG. 18. A thin mandrel or other object such asa pin may be placed through noose 194 to maintain patency. Sliding knot198, such as a bunt line half hitch knot, is tied in close proximity tothe noose 194 and the suture is placed in sliding engagement withfeature 207 of anchor 205. Sliding knot 198 is then dressed or finalizedas desired.

Conventionally, rotator cuff lateral row fixation involves spanning asuture bridge from medial anchors. Sutures are fixated with knotted orknotless anchors at the lateral row. Unthreaded anchors suffer moreoften than threaded anchors from anchor pull out, and suture slippagemay occur at relatively low loads in many conventional proceduresregardless of anchor type.

A presently preferred technique for rotator cuff double row repair isillustrated in FIGS. 22-27 utilizing the snare assembly of FIG. 18.Medial row anchor 240, FIG. 22, is shown already embedded in bone Bhaving cuff tissue T fixated at the medial row with suture 242.Preferably, a threaded anchor is utilized for anchor 240, and may be thesame type of anchor as anchor 205. Free suture limbs 244 and 246 areretracted out of the joint space, shown in FIG. 22 as extending beyondskin S. Threaded anchor 205, FIG. 23 is then placed as a lateral rowanchor in hole H independently of the medial row fixation. At thisstage, collapsible loop 200 is long enough to enable sliding knot 198and noose loop 194 to extend out of the joint space.

Suture limbs 244, 246 from the medial row are then passed through noose194, FIG. 24, preferably utilizing one of the threader devices describedabove. Any tension on suture limbs 244, 246 will collapse noose 194around them. The size of the threader tube may be selected to limit themigration of noose 194 from sliding knot 198. Post limb 206 is thentensioned, FIG. 25, in the proximal direction indicated by arrow 250 toretract sliding knot 198 into or in close proximity to anchor 205 and toplace initial tension on suture bridge 258.

A simple knot such as a half hitch is then tied between suture limbs244, 246 and pushed down against noose 194, FIG. 26, as sliding knot 260while limbs 244 and 246 are pulled to further tension suture bridge 258as desired. As second or more half hitches 262, FIG. 27, are added aftersuture bridge 258 has been properly tensioned to permanently lock therepair and the ends of suture limbs 244 and 246 are trimmed. Because asingle noose can handle multiple pairs of sutures as described above inrelation to FIG. 20, additional suture bridges can be secured frommultiple medial anchors as desired.

Adjustable suture snare assembly 310, FIG. 28, has a suture anchor 312and a closed, fixed-length loop 306 of a first material 302, which has anoose 304 tied at one end. A half hitch “pretzel”-like knot 305 is shownin this construction; another construction having a unitary fixed loopis disclosed in U.S. patent application Ser. No. 12/977,146 (Hernandezet al.), which is incorporated herein by reference. Loop 306 is capturedby, in other words, is connected to, a second filament 316 having aterminal end 318, a post limb 320, a sliding bunt line half hitch knot322, and an adjustable loop 324 with loop limbs 326 and 328. Secondfilament 316 may be considered as part of an adjustable filamentengagement feature of anchor 12, because filament 316 connects noose 304to anchor 12. In one construction, suture anchor 312 is similar to thecannulated suture anchor disclosed by Cauldwell et al. in U.S. PatentApplication Publication No. 2008/0147063, incorporated herein byreference. In anchor systems utilized according to this sliding knotconfiguration of the present invention, however, it is not necessary tohave a post-like suture-engaging member or other occluding element overwhich one or more sutures or suture limbs pass to serve as a restrictionto proximal movement; in many constructions, it is sufficient to have arestricted opening 346 to prevent withdrawal of knot 322.

Suture anchor 312 has a proximal end 330 and a distal end 332 withopposed distal arms 334 and 336 defining cut-out 338 between them.Passage 340 is an inner lumen which runs from proximal end 330 to distalcut-out 338. Although knot 322 is shown extending beyond cut-out 338 inFIG. 28 for purposes of illustration, knot 322 preferably is seatedagainst restricted opening 346 between arms 334 and 336, or otherwisemaintained at the distal end 332 by a cavity or other feature, duringinsertion of snare assembly 310 into a patient to minimize interferenceby the knot 322 with the bone-engaging feature 342, or other exteriorsurface of anchor 312, and the bone in which suture anchor 312 isfixated.

One or more bone-engaging features 342, such as the helical threadillustrated in FIG. 28 or other features such as teeth, ridges, or otherprotrusions, are formed on the exterior of anchor 312 to enhancefixation in bone. Threads such as found on the Healix™ anchor availablefrom DePuy Mitek Inc. are desirable. In another construction, the sutureanchor rotates to toggle into bone at its proximal end to minimizewithdrawal. In a number of constructions, a hole is formed in bone priorto anchor insertion; in other constructions, a suture anchor is inserteddirectly into bone. Further, one or more passages or channels may beformed on the exterior of the suture anchor, such as channel 344illustrated in phantom, FIG. 28, traversing bone-engaging element 342.

It is a matter of surgeon preference whether a terminal end 318 is keptat a length sufficient to lie against the exterior of at least onebone-engaging feature 342 to be trapped against bone during insertion,or is trimmed to a shorter length. Further, a restriction such asrestricted opening may be defined at least in part by engagement withbone when anchor 312 is fixated in bone to prevent knot 322 from movingwith post limb 320 when tension is applied to post limb 320.

One or more such distal extensions or other protrusions may be provided,similar in some constructions to Cauldwell et al. cited above or to U.S.Pat. No. 7,381,213 by Lizardi, also incorporated herein by reference. Inyet other constructions, a cylindrical or otherwise circumferentialcavity, bowl or countersink feature is provided at the distal end of theanchor to seat the knot 322 during insertion and fixation.

Slidable knot 322 has been described as a bunt line half hitch knot insome constructions, but other suitable knots will be readily apparent tothose of ordinary skill in the suture tying art after reviewing thepresent invention. The term “slidable” as used herein is intended toinclude slidable, lockable knots as well as slidable knots, such asthose described in the Arthroscopic Knot Tying Manual (2005) availablefrom DePuy Mitek, as well as the slidable, lockable knot by Wenstrom,Jr. in U.S. Pat. No. 6,767,037.

Several improvements according to the present invention are illustratedin FIGS. 29-50. A filament 400, FIG. 29, has a noose 402 and noose limbs404 and 406. Noose 402 defines a central opening 408 and secondaryopenings 410 and 412 formed from a half hitch plus one additional throwof limb 406 through central opening 408. A flexible sleeve 414 is shownin phantom encapsulating some of limbs 404 and 406 in certainconstructions, as described in more detail below.

FIGS. 30-31 illustrate the formation of a cinch noose 420, also referredto as an improved cinch noose construct, having an opening 422. The endsof free filament limbs 424 and 426 of filament 400 are passed throughcentral opening 408, as represented by arrows 427 and 429 in FIG. 30,which draws noose limbs 424 and 426 therethrough. Noose 402 is thentightened, FIG. 31, to form a slidable knot for cinch noose 420.Alternatively, if a sleeve 414, FIG. 29, or sleeve 414 a, FIG. 31, isnot utilized, or if such sleeve is removed after being passed throughtissue to be tensioned, then one or both of free limbs 424, 426 can bepassed through one or both of openings 410, 412. One technique forutilizing improved cinch noose 420 is described below regarding FIGS.34-40.

Filament 400 with noose 402, FIG. 29, is shown in FIG. 32 slidablyconnected with anchor 430 as a snare assembly 432, after placementthrough skin S into bone B of a patient. Sleeve 414 is positioned overand encapsulates the entire portion of first and second free limbs 424,426, down substantially to, but not into, anchor 430 in thisconstruction.

It is a realization of the present invention that joining together atleast the free filament limbs improves suture management and reduces thepossibility of suture entanglement or damage by instruments, especiallywhen passed through a cannula. For example, a surgeon or other user needonly grasp and pass one sleeve 414 through noose 402 to therebymanipulate free filament limbs 424, 426 as a single unit. Additionalconvenience can be provided by perceptible indicators on one or moresleeves such as different markings, colors, diameters, braid or designpatterns, or other tactile or visual indicia, especially if multipletissue attachments or anchors are utilized, such as described above inrelation to FIG. 20. Preferably, the sleeves are removed and discardedafter the filaments have been manipulated, as described below, so theperceptible indicators do not need to meet long-term implantationrequirements.

One technique for calculating the relative lengths of filament 501 andsleeve 508 is illustrated in FIG. 33 for snare assembly 500 according tothe present invention. A first factor is the distance, represented byarrow 502, between noose 504, in a substantially collapsed or reducedcondition, and the distal end 506 of sleeve 508 over noose limbs 503 and505. One goal is to have distal end 506 accessible outside of a cannulaafter tissue is tensioned to enable latching or snagging of distal end506 by a knot pusher or grasper to facilitate removal of sleeve 508, asdescribed in more detail below for other sleeves. Typical cannulalengths for hip and shoulder surgeries are between four to six inches,and the cannulas are typically placed approximately one-half inch frombone. The length of anchor 510 is included in the calculation.

For some constructions prior to implantation in a patient, sleeve 508 istwenty five inches in total length, with seven and one-half inchesextending from the filament engagement feature of anchor 510 towardnoose 504 as indicated by arrow 512, with seventeen and one-half inches,arrow 514, extending over and beyond free filament limbs 513 and 515 toproximal end 516 of sleeve 508. In one construction, filament 501 has atotal length of thirty six inches, or a folded length of eighteeninches, with sixteen and one-half inches, arrow 520, extending fromnoose 504 to anchor 510, and one and one-half inches, arrow 522, as freelimbs 513 and 515. In another construction wherein filament 501 has atotal length of sixty six inches and a folded length of thirty threeinches, free filament limbs 513, 515 extend sixteen and one-half inch asrepresented in phantom by arrow 524. In either construction, marks canbe placed on the filament noose limbs 503, 505 nine inches from thecenter or middle, where noose 504 will be formed, to clearly indicatethe proper positioning, arrows 502 and 512, of distal end 506 of thesleeve 508 over filament 501 during preparation of snare assembly 500for implantation.

A technique for utilizing the improved cinch noose 420, FIG. 31, with asleeve 414 a is shown in FIGS. 34-40 for another embodiment, representedby snare assembly 530 according to the present invention. In thisconstruction, the sleeve 414 a, shown with dashed lines, is slid overfilament 400 a and then loaded through anchor 532 to cover all of freelimbs 424 a, 426 a and at least some of noose limbs 404 a, 406 a,preferably covering all of noose limbs 404 a, 406 a as they emerge abovea cannula (not shown) passing through skin S during initial implantationof anchor 532 in bone B, FIG. 34 to assist in suture management andprotection.

The proximal end of sleeve 414 a is passed through tissue T, FIG. 35,and then passed through cinch noose 420 a, FIG. 36. Alternatively,sleeve 414 a can be removed after it is passed through noose 420 a sothat free limbs 424 a and 426 a can be passed directly through one ormore openings in noose 420 a. In either scenario for FIG. 36, the noose420 a is then dressed, that is, collapsed, FIG. 37, and then advancednear tissue T and tightened, FIG. 38. The sleeve 414 a is then removedentirely, FIG. 39, and discarded according to standard procedures. Thetissue repair is then finished with one or more half hitches 534 asdesired, FIG. 40.

Materials for sleeves include braided sutures such as Ethibond™ size 0suture or Orthocord™ size 2 suture, also referred to as Orthocord™ #2suture, which is typically braided at sixty picks per inch. For use as asleeve, a more relaxed braid of approximately thirty to forty picks perinch is preferred, more preferably about 36 picks per inch. If thesleeve material is formed about a core, preferably that core is removedto facilitate insertion of the filament limbs, which may themselves beformed of typical suture such as Orthocord™ #0 suture or #2 suturebraided at sixty picks per inch.

In yet another sleeve embodiment according to the present invention, oneof the free filament limbs itself serves as the sleeve. For theconstruction illustrated in FIG. 41, snare assembly 540 has a filament542 of Orthocord™ #2 suture generally braided at sixty picks per inchwith a noose 544 and noose limbs 545 and 546 that pass around filamentengagement feature 550 of anchor 548. Noose limbs 545 and 546 becomefree filament limbs 555 and 556, respectively, extending proximally. Atpoint 558, however, a proximal section of limb 555 is braided at fewerpicks per unit length, preferably more than ten percent fewer, morepreferably at least twenty five percent fewer, to serve as sleeve 560extending to its proximal end 562. The other free filament limb 556 isthreaded through sleeve 560 to emerge as proximal end 564 in thisconstruction; in other constructions, the proximal end 564 lies whollywithin sleeve 560.

One technique for constructing snare assembly 540 is illustrated inFIGS. 42A-42D. Filament 542 is shown in FIG. 42A as initiallymanufactured with sleeve 560 being a section of suture formed with fewerpicks per inch beginning at point 558 and extending to end 562,preferably reduced from the standard 60 picks per inch to 36 picks perinch in this construction. Noose 544 is then created, FIG. 42A, and thenfilament ends 562, 564 are threaded through anchor 548 as shownschematically in FIG. 42C. After a core element within sleeve section560 has been removed, filament end 564 is then threaded within sleeve560 using a needle-type insertion device to achieve snare assembly 540,FIG. 42D, with coaxial filament limbs in the sleeve section 560. Thelength of sleeve 560 is likely to decrease as its diameter is expandedby the insertion device.

One procedure for utilizing snare assembly 540 is shown in FIGS. 43-45.Anchor 548 is inserted into bone B, FIG. 43, and then coaxial sleevesection 560 is passed through tissue T, FIG. 44, and then noose 544,FIG. 45. Noose 544 is then collapsed toward tissue T, FIG. 46, sleeve560 is severed from filament 542, and then filament 542 is tied and cutas described above for other embodiments to finish fixation of tissue T.The excess portion of filament 542, including coaxial sleeve section560, is discarded.

Another embodiment according to the present invention is illustrated inFIGS. 47-50. Snare assembly 570 has a fixed-length, preferablycontinuous loop 572 of a first filament which a surgeon or other userutilizes to form a Lark's Head knot, also known as a Bale Sling Hitch,to serve as a noose 573, FIG. 48, to grip a section of a second filament574 as shown in FIGS. 49-50.

Second filament 574, FIG. 47, has a collapsible loop 578 with a slidingknot 576 such as a sliding bunt line half hitch knot, a tensioning orpost limb 580, and a tag or terminal limb 581. Collapsible loop 578passes around filament engagement feature 592, also referred to as asaddle 592, of bone anchor 590. In one construction, snare assembly 570is manufactured in the condition shown in FIG. 47 and supplied to a userwith sliding knot 576 already tied. To utilize snare assembly 570, ahole 594 is formed in bone B and the anchor 590 is inserted to theposition shown in FIG. 47, and then continuous loop 572 is passedthrough tissue T.

After the noose 573 is formed with a Lark's Head knot, tail 580 andsliding knot 576 are passed through noose 573, FIG. 49. Noose 573 isthen tightened against sliding knot 576. A knot pusher 596, FIG. 50,assists in collapsing the loop 578 to tighten the snare assembly 570 toapply tension to tissue T. Depending on the overall length of first loop572, a portion of it may be drawn into anchor 590.

Thus, when snare assembly 570 is supplied to a surgeon or other userwith sliding knot 576 already tied, snare assembly 570 serves anotherexample according to the present invention of a pre-formed, knot-lessfilament system which does not require the user to manipulate free limbsto tie knots during an operation. Adding to the benefits of snareassemblies according to the present invention, including high strengthand loop security, low knot profile, ability to tension incrementally,and easy use with threaded anchors, providing a loop capable of forminga Lark's Head removes altogether the burden of tying a knot near orwithin a patient.

In other words, a first filament, preferably a continuous fixed-lengthsuture loop, is slidably attached to a collapsible filament loop of asecond filament having a preformed sliding knot. In another constructionshown in FIG. 48A, the fixed-length loop 572 a is formed at one end of afirst filament 601, such as by pre-tying a first bowline knot 600, andthe other end of the first filament 601 is slidably attached to thesecond filament 574 a with another, smaller loop 603, such as formed bya second, smaller pre-tied bowline knot 602 through which thecollapsible loop 578 a passes. After the anchor is placed in bone, thecontinuous-loop end with bight 575 a is passed through tissue. A Lark'sHead knot is then created on the continuous loop 572 a, which generatesa very robust noose.

One or more tools can be utilized to assist creation of the constructsdescribed above, especially if a half hitch is desired to be thrown onfree filament limbs passing through different loops of a “pretzel”noose, that is, a noose with at least one half hitch that definesmultiple loops through which the free filament limbs are passed.Improved threading tools and suture passers are illustrated in FIGS.51-57 to automatically create a simple half hitch when two filament endsare pulled through loops of a noose.

Suture passer 620 is shown in FIG. 51 placed diagonally over suturepasser 610. Suture passer 610 has proximal tab or handle 612, shaft 614formed of wire or other flexible material, and opening 615 at distal end616. Suture passer 620 has proximal handle 622, flexible shaft 624, andan opening 625 at distal end 626. Distal end 626 is looped under andaround shaft 614 to create a simple half hitch 630, FIG. 52.

Intertwined suture passers 610 and 620 are shown held by threader tool700 in FIG. 53. Tool 700 has projections 702 and 704 which aresubstantially cylindrical tubes in this construction, whose distal endsare similar to tubes 102 and 104 of FIGS. 14A-14B above. Each projection702, 704, FIGS. 53-53A, is supported by common handle 703 and has alongitudinal channel 706, 708, respectively, with slots 710, 712 tofacilitate placement of filaments or passers such as suture passers 610,620 into tool 700, and to facilitate subsequent removal of filamentsdrawn into tool 700 by the passers. Tool 700 further defines a commonpassage 720, formed in part by notches in the proximal walls ofprojections 702 and 704, which interconnects the proximal portions ofchannels 706 and 708. Half hitch 630, FIG. 52, lies within passage 720,FIG. 53, and is further held by fixed stop 730 with lip or overhang 732,which is an inverted “L” shape in this construction. Tool 700 furtherincludes a distal finger 740 in this construction to serve as a catch orpost for one or more filaments during the threading procedure, such asto hold a cinch loop or other noose in position.

In another construction shown in side view in FIG. 54, a tool 700 a hasa movable stop 730 a with a strut 734 a pivotally attached to handle 703a by pin 740 passing through the lower portion of strut 734 a, or othertype of hinge such as a living hinge. Tubular projection 702 a isvisible in this view. Stop 730 a has a lip 732 a supported by strut 734a. In one construction, a user manipulates stop 730 a to hold or releasesuture passers by moving stop 730 a toward or away from handle 703 a asindicated by arrow 736; stop 730 a is shown in phantom in an openposition after being moved away from handle 703 a. In anotherconstruction, a spring 742, also shown in phantom, biases stop 730 a inone direction, preferably toward handle 703 a. As a user pulls suturethrough the device, a certain amount of force causes stop 730 a toovercome the biasing force of spring 742 and move away from handle 703 ato assist release of the tied suture.

Several threader tools according to the present invention havingintersecting channels are shown in top view in FIGS. 55-57. A V-shapedtool 800, FIG. 55, has projections 802, 804 with intersecting channels806 and 808, respectively, and a distal finger 840. A proximaltrapezoidal stop 830 holds suture passers in place as they pulledproximally. The distal portions of projections 802, 804 becomesubstantially parallel to each other to assist removal of the tied knotfrom tool 800.

Tool 900, FIG. 56, has straight projection 902 and curved projection 904that define channels 906 and 908, respectively. Stop 930 forms aproximal corner at the intersection where sutures can be pulledproximally when force is applied at right angles to respective suturepassers, which is expected to ease suture movement through the channels906, 908.

Tool 1000, FIG. 57, is a horseshoe shape to reduce forces needed to pullsutures through the tool 1000. Finger 1040 is positioned slightly belowto distal opening of channels 1006, 1008 to minimize obstruction of thesuture threading process.

This invention may also be expressed as a surgical filament snareassembly with a bone anchor and a first filament having a noose, formedfrom at least one half hitch, on a first portion of at least a firstlimb and having a second portion connected to the filament engagementfeature of the anchor. The noose is capable of receiving at least twofree filament limbs and strangulating them when tension is applied to atleast one of the free filament limbs and the noose. Preferably, theassembly further includes a threader tool having at least twoprojections having distal ends capable of being removably inserted intodifferent loops of the half hitch. Each projection defines a channelcapable of receiving a portion of at least one free filament limb topass it through a loop of the half hitch, and each projection furtherdefines a slot communicating with the channel to facilitate removal ofthe filament limb from the tool. Each slot has the same width as itscorresponding channel in some embodiments and, in other embodiments, hasa different width, typically a narrower width, than that of thecorresponding channel.

In certain embodiments, the projections are tubes joined together withat least one handle for manipulation the tube. The proximal ends of thechannels are connected by one of an intersection and a common passage,and the tool further includes a stop as a proximal portion of the one ofthe intersection and the common passage. In some embodiments, the stopis movable, and may include a spring to bias the stop toward theintersection or common passage.

In yet other embodiments, the assembly further includes at least twosuture passers having distal ends for engaging portions of the freefilament limbs, and the suture passers being capable of pulling the freefilament limbs through the channels when proximal-directed force isapplied to proximal ends of the suture passers. Preferably, the distalends of the suture passers are intertwined in at least one half hitch toimpart at least one half hitch to the free filament limbs when they aredrawn through the tool. Different combinations selected from the groupof an anchor, one or more filament constructs as described herein, athreader tool, and one or more suture passers can also be referred to asdifferent kits according to the present invention.

Thus, while there have been shown, described, and pointed outfundamental novel features of the invention as applied to a preferredembodiment thereof, it will be understood that various omissions,substitutions, and changes in the form and details of the devicesillustrated, and in their operation, may be made by those skilled in theart without departing from the spirit and scope of the invention. Forexample, it is expressly intended that all combinations of thoseelements and/or steps that perform substantially the same function, insubstantially the same way, to achieve the same results be within thescope of the invention. Substitutions of elements from one describedembodiment to another are also fully intended and contemplated. It isalso to be understood that the drawings are not necessarily drawn toscale, but that they are merely conceptual in nature. It is theintention, therefore, to be limited only as indicated by the scope ofthe claims appended hereto.

Every issued patent, pending patent application, publication, journalarticle, book or any other reference cited herein is each incorporatedby reference in their entirety.

What is claimed is:
 1. A surgical repair method, comprising: selecting asurgical filament assembly comprising: a slidable knot having on oneside thereof a cinch noose loop defined by a first filament and a secondfilament, the slidable knot having on the other side thereof first andsecond filament limbs; and a flexible sleeve removably encapsulating atleast a portion of the first and second filament limbs; fixing an anchorin bone in proximity to detached soft tissue; passing a first end ofeach of the first and second filament limbs through a portion of thedetached soft tissue and around an engagement feature of the anchor suchthat the cinch noose loop extends from one side of the anchor and thesleeve extends from another side of the anchor; passing the first end ofeach of the first and second filament limbs through the cinch nooseloop; collapsing the cinch noose loop around the first and secondfilament limbs disposed therethrough to engage the soft tissue; andadvancing the collapsed cinch noose loop distally to bring the tissueinto proximity with the bone.
 2. The method of claim 1, furthercomprising applying one or more knots proximate to the collapsed cinchnoose loop following the advancing step to maintain the tissue at adesired location in proximity to the bone.
 3. The method of claim 1,wherein proximal portions of the first ends of the first and secondfilament limbs are encapsulated in the flexible sleeve when the firstand second filament limbs are passed through the tissue.
 4. The methodof claim 3, wherein passing the first end of each of the first andsecond limbs through the opening of the cinch noose loop furthercomprises passing at least a portion of the sleeve through the cinchnoose loop.
 5. The method of claim 4, wherein advancing the collapsedcinch noose loop comprises advancing the collapsed cinch noose loop pasta distal-most end of the flexible sleeve, and the method furthercomprises removing the flexible sleeve from the first and secondfilament limbs.
 6. The method of claim 1, wherein a distal end of thesleeve terminates prior to a proximal end of the anchor.
 7. The methodof claim 1, wherein the sleeve is slidably disposed around a portion ofthe filament engagement feature such that the sleeve extends from bothsides of the anchor.
 8. The method of claim 1, further comprises passingat least one of a first end of the surgical filament assembly and asecond end of a surgical filament assembly through a surgical cannula.9. The method of claim 1, wherein the passing, collapsing, and advancingsteps are effected without tying a knot in the first or second filamentsor in the first and second filament limbs.